{"url_path":"/fda/drug/recalls/D-0653-2026","section_key":"summary","section_title":"DRUG Recall: ACCORD BIOPHARMA INC — IMULDOSA, (ustekinumab-srlf) Injection, 130 mg/26 mL (5mg/mL), Rx only, Single dose vial, Manufactured by Accord BioPharma Inc., 8041 Arco corporate Drive, Suite 200, Raleigh, NC 27617, USA, Manufactured at: Catalent Indiana, LLC, 1300 S. Patterson Drive, Bloomington, IN 47403, USA, NDC 69448-019-26.","topic":"fda","document":{"doc_type":"drug-recall","doc_date":"2026-06-10","source_url":"https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0653-2026%22","accession_number":null,"cik":null,"ticker":null,"issuer_name":null,"edgar_url":null,"primary_entity_key":null,"primary_entity_name":"ACCORD BIOPHARMA INC"},"word_count":88,"has_tables":false,"body_markdown":null}